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Volumn 128, Issue 10, 2006, Pages 3150-3151

Cationic shape-persistent macrocycles: The unexpected formation of a nano-size supramolecular dimer

Author keywords

[No Author keywords available]

Indexed keywords

BROMIDE; CALIXARENE; CATION; COPOLYMER; CYCLOHEXANE; DICHLOROMETHANE; DIMER; MACROCYCLIC COMPOUND; PHENYL GROUP; PYRIDINE DERIVATIVE; TETRAHYDROFURAN;

EID: 33644950243     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja057999g     Document Type: Article
Times cited : (42)

References (24)
  • 1
    • 0000963686 scopus 로고    scopus 로고
    • For recent reviews on shape-persistent macrocycles, mainly phenylene ethynylene-based, see: (a) Moore, J. S. Acc. Chem. Res. 1997, 30, 402-413.
    • (1997) Acc. Chem. Res. , vol.30 , pp. 402-413
    • Moore, J.S.1
  • 12
    • 0344012946 scopus 로고    scopus 로고
    • +-induced tubular self-assembly of Schiff-base macrocycles but not investigated in detail: Gallant, A. J.; MacLachlan, M. J. Angew. Chem., Int. Ed. 2003, 42, 5307-5310.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5307-5310
    • Gallant, A.J.1    MacLachlan, M.J.2
  • 22
    • 33644932812 scopus 로고    scopus 로고
    • note
    • MM calculations have shown that the boat and chair conformations of shape-persistent phenylene ethynylene macrocycles of this type are energetically slightly favored over the planar conformation (ref 7). A computational analysis explaining at a molecular level the preference of 2 for dimerization over oligomerization is in progress.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.